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In Situ Synthesis of a Magnetic Graphene Platform for the Extraction of Benzimidazoles from Food Samples and Analysis by High-Performance Liquid Chromatography

A novel method was proposed for the determination of five benzimidazoles (oxfendazole, mebendazole, flubendazole, albendazole, and fenbendazole) using magnetic graphene (G-Fe(3)O(4)). G-Fe(3)O(4) was synthesized via in situ chemical coprecipitation. The properties of G-Fe(3)O(4) were characterized b...

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Detalles Bibliográficos
Autores principales: Zhang, Qianchun, Liu, Yulan, Wang, Xingyi, Li, Huimin, Chen, Junyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435904/
https://www.ncbi.nlm.nih.gov/pubmed/28546882
http://dx.doi.org/10.1155/2017/3018198
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author Zhang, Qianchun
Liu, Yulan
Wang, Xingyi
Li, Huimin
Chen, Junyu
author_facet Zhang, Qianchun
Liu, Yulan
Wang, Xingyi
Li, Huimin
Chen, Junyu
author_sort Zhang, Qianchun
collection PubMed
description A novel method was proposed for the determination of five benzimidazoles (oxfendazole, mebendazole, flubendazole, albendazole, and fenbendazole) using magnetic graphene (G-Fe(3)O(4)). G-Fe(3)O(4) was synthesized via in situ chemical coprecipitation. The properties of G-Fe(3)O(4) were characterized by various instrumental methods. G-Fe(3)O(4) exhibited a great adsorption ability and good stability towards analytes. Various experimental parameters that might affect the extraction efficiency such as the amount of G-Fe(3)O(4), extraction solvent, extraction time, and desorption conditions were evaluated. Under the optimized conditions, a method based on G-Fe(3)O(4) magnetic solid-phase extraction coupled with high-performance liquid chromatography was developed. A good linear response was observed in the concentration range of 0.100–100 μg/L for the five benzimidazoles, with correlation coefficients ranging from 0.9966 to 0.9998. The limits of detection (S/N = 3) of the method were between 17.2 and 32.3 ng/L. Trace benzimidazoles in chicken, chicken blood, and chicken liver samples were determined and the concentrations of oxfendazole, mebendazole, flubendazole, and fenbendazole in these samples were 13.0–20.2, 1.62–4.64, 1.94–6.42, and 0.292–1.04 ng/g, respectively. The recovery ranged from 83.0% to 115%, and the relative standard deviations were less than 7.9%. The proposed method was sensitive, reliable, and convenient for the analysis of trace benzimidazoles in food samples.
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spelling pubmed-54359042017-05-25 In Situ Synthesis of a Magnetic Graphene Platform for the Extraction of Benzimidazoles from Food Samples and Analysis by High-Performance Liquid Chromatography Zhang, Qianchun Liu, Yulan Wang, Xingyi Li, Huimin Chen, Junyu J Anal Methods Chem Research Article A novel method was proposed for the determination of five benzimidazoles (oxfendazole, mebendazole, flubendazole, albendazole, and fenbendazole) using magnetic graphene (G-Fe(3)O(4)). G-Fe(3)O(4) was synthesized via in situ chemical coprecipitation. The properties of G-Fe(3)O(4) were characterized by various instrumental methods. G-Fe(3)O(4) exhibited a great adsorption ability and good stability towards analytes. Various experimental parameters that might affect the extraction efficiency such as the amount of G-Fe(3)O(4), extraction solvent, extraction time, and desorption conditions were evaluated. Under the optimized conditions, a method based on G-Fe(3)O(4) magnetic solid-phase extraction coupled with high-performance liquid chromatography was developed. A good linear response was observed in the concentration range of 0.100–100 μg/L for the five benzimidazoles, with correlation coefficients ranging from 0.9966 to 0.9998. The limits of detection (S/N = 3) of the method were between 17.2 and 32.3 ng/L. Trace benzimidazoles in chicken, chicken blood, and chicken liver samples were determined and the concentrations of oxfendazole, mebendazole, flubendazole, and fenbendazole in these samples were 13.0–20.2, 1.62–4.64, 1.94–6.42, and 0.292–1.04 ng/g, respectively. The recovery ranged from 83.0% to 115%, and the relative standard deviations were less than 7.9%. The proposed method was sensitive, reliable, and convenient for the analysis of trace benzimidazoles in food samples. Hindawi 2017 2017-05-04 /pmc/articles/PMC5435904/ /pubmed/28546882 http://dx.doi.org/10.1155/2017/3018198 Text en Copyright © 2017 Qianchun Zhang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Qianchun
Liu, Yulan
Wang, Xingyi
Li, Huimin
Chen, Junyu
In Situ Synthesis of a Magnetic Graphene Platform for the Extraction of Benzimidazoles from Food Samples and Analysis by High-Performance Liquid Chromatography
title In Situ Synthesis of a Magnetic Graphene Platform for the Extraction of Benzimidazoles from Food Samples and Analysis by High-Performance Liquid Chromatography
title_full In Situ Synthesis of a Magnetic Graphene Platform for the Extraction of Benzimidazoles from Food Samples and Analysis by High-Performance Liquid Chromatography
title_fullStr In Situ Synthesis of a Magnetic Graphene Platform for the Extraction of Benzimidazoles from Food Samples and Analysis by High-Performance Liquid Chromatography
title_full_unstemmed In Situ Synthesis of a Magnetic Graphene Platform for the Extraction of Benzimidazoles from Food Samples and Analysis by High-Performance Liquid Chromatography
title_short In Situ Synthesis of a Magnetic Graphene Platform for the Extraction of Benzimidazoles from Food Samples and Analysis by High-Performance Liquid Chromatography
title_sort in situ synthesis of a magnetic graphene platform for the extraction of benzimidazoles from food samples and analysis by high-performance liquid chromatography
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435904/
https://www.ncbi.nlm.nih.gov/pubmed/28546882
http://dx.doi.org/10.1155/2017/3018198
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